RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

Published:2016-10-13 Issue:10 Volume:11 Page:e0164759
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Kobayashi Hatasu,Brozman Miroslav,Kyselová Kateřina,Viszlayová Daša,Morimoto Takaaki,Roubec Martin,Školoudík David,Petrovičová Andrea,Juskanič Dominik,Strauss Jozef,Halaj Marián,Kurray Peter,Hranai Marián,Harada Kouji H.,Inoue Sumiko,Yoshida Yukako,Habu Toshiyuki,Herzig Roman,Youssefian Shohab,Koizumi Akio

Funder

Japan Society for the Promotion of Science (JP)

Japan Society for the Promotion of Science

Ministry of Health, Labour and Welfare

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference14 articles.

1. Hypoplasia of bilateral internal carotid arteries. (in Japanese);K Takeuchi;Brain Nerve,1957

2. Spontaneous occlusion of the circle of Willis. A disease apparently confined to Japanese;T Kudo;Neurology,1968

3. Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain;J Suzuki;Arch Neurol,1969

4. Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development;W Liu;PLoS One,2011

5. A genome-wide association study identifies RNF213 as the first Moyamoya disease gene;F Kamada;J Hum Genet,2011

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. RNF213 in moyamoya disease: Genotype–phenotype association and the underlying mechanism;Chinese Medical Journal;2024-01-19

2. Yield of genetic evaluation in non-syndromic pediatric moyamoya patients;Child's Nervous System;2023-10-01

3. Difference in Clinical Phenotype, Mutation Position, and Structural Change of RNF213 Rare Variants Between Pediatric and Adult Japanese Patients with Moyamoya Disease;Translational Stroke Research;2023-09-28

4. RNF213 p.R4810K variant in moyamoya disease in adults and children from a Malaysian tertiary center;Neurology Asia;2023-09

5. Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study;Brain and Spine;2023

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3